Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.21200620A= , CM000674.2:g.21200620A= | GRCh38 |
| NC_000012.11:g.21353554A= , CM000674.1:g.21353554A= | GRCh37 |
| NC_000012.10:g.21244821A= | NCBI36 |
| NG_011745.1:g.74427A= , LRG_1022:g.74427A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000256958.3:c.1083A= MANE Select | ENSP00000256958.2:p.Lys361= | |
| ENST00000256958.2:c.1083A= | ENSP00000256958.2:p.Lys361= | |
| NM_006446.4:c.1083A= , LRG_1022t1:c.1083A= | NP_006437.3:p.Lys361= | |
| NM_006446.5:c.1083A= MANE Select | NP_006437.3:p.Lys361= |